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Results 1 - 3 of 3 for DEXTROSE OR FRUCTOSE OR PHOSPHORIC ACID
  1. ALDOB gene 
    ... found in approximately half of people with hereditary fructose intolerance replaces the amino acid alanine with the amino acid proline at position 149 in the enzyme (written as Ala149Pro or A149P). This mutation alters the ... B cannot metabolize fructose.A lack of functional aldolase B results in ...
    https://medlineplus.gov/genetics/gene/aldob - Genetics
  2. Where can I read more about the diseases and traits covered in my direct-to-consumer genetic testing report?: ... 
    ... Gaucher disease Glycogen storage disease type I Hereditary fructose intolerance Junctional epidermolysis bullosa Leigh syndrome Limb-girdle ... hyperoxaluria Pyruvate kinase deficiency Rhizomelic chondrodysplasia punctata Sialic acid storage disease , including Salla disease Sickle cell disease , ...
    https://medlineplus.gov/.../dtcgenetictesting/dtcghrpages - Genetics
  3. GPI gene 
    ... 6-phosphate is converted to another molecule called fructose-6-phosphate.When GPI remains a single molecule ( ... GPI deficiency replace single protein building blocks (amino acids) in the GPI enzyme. Some of these mutations ...
    https://medlineplus.gov/genetics/gene/gpi - Genetics